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Correlation of fast and slow chemical shift spinning sideband patterns under fast magic-angle spinning.

作者信息

Eléna Bénédicte, Hediger Sabine, Emsley Lyndon

机构信息

Laboratoire de Stéréochimie et des Interactions Moléculaires, UMR 5532, CNRS/ENS Lyon, France.

出版信息

J Magn Reson. 2003 Jan;160(1):40-6. doi: 10.1016/s1090-7807(02)00037-x.

DOI:10.1016/s1090-7807(02)00037-x
PMID:12565047
Abstract

A new two-dimensional solid-state NMR experiment, which correlates slow and fast chemical shift anisotropy sideband patterns is proposed. The experiment, dubbed ROSES, is performed under fast magic-angle spinning and leads to an isotropic spectrum in the directly detected omega(2) dimension. In the evolution dimension omega(1), the isotropic chemical shift is reduced by a factor S, and spinning sidebands are observed spaced by a scaled effective spinning speed omega(R)/S. These spinning sidebands patterns are not identical to those observed with standard slow magic-angle spinning experiments. Chemical shift anisotropy parameters can be accurately extracted with standard methods from these spinning sideband patterns. The experiment is demonstrated with carbon-13 experiments on powdered samples of a dipeptide and a cyclic undecapeptide, cyclosporin-A.

摘要

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